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高时间分辨率转录谱分析揭示大鼠坐骨神经恢复过程中强烈的免疫/炎症反应。

Transcriptional Profiling at High Temporal Resolution Reveals Robust Immune/Inflammatory Responses during Rat Sciatic Nerve Recovery.

作者信息

Xing Lingyan, Cheng Qiong, Zha Guangbin, Yi Sheng

机构信息

Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong 226001, China.

出版信息

Mediators Inflamm. 2017;2017:3827841. doi: 10.1155/2017/3827841. Epub 2017 Apr 12.

Abstract

After peripheral nerve injury, immune/inflammatory responses are triggered, which are critical for nerve regeneration. Despite their importance, the underlying molecular changes in immune/inflammatory responses remain largely unknown. In this study, we systematically analyzed differentially expressed genes in immune/inflammatory-related pathways at high temporal resolution and experimentally validated gene expression changes with RT-PCR following sciatic nerve crush in rats. We found that immune/inflammatory reactions not only occur in the acute injury but also remained activated over two weeks after injury. Detailed bioinformatic studies suggested that multiple immune/inflammatory pathways, including agranulocyte adhesion and diapedesis, granulocyte adhesion and diapedesis, IL-6 signaling, and IL-10 signaling, were sustained activated during nerve degeneration and regeneration. Our current study expands our understanding of the molecular basis of altered immune/inflammatory-related pathways following injury and thus might offer the possibility of targeting related molecules as therapeutic intervention for peripheral nerve regeneration.

摘要

周围神经损伤后,免疫/炎症反应被触发,这对神经再生至关重要。尽管它们很重要,但免疫/炎症反应中潜在的分子变化仍 largely 未知。在本研究中,我们以高时间分辨率系统分析了免疫/炎症相关途径中差异表达的基因,并在大鼠坐骨神经挤压伤后用 RT-PCR 实验验证了基因表达变化。我们发现免疫/炎症反应不仅发生在急性损伤期,而且在损伤后两周内仍保持激活状态。详细的生物信息学研究表明,多种免疫/炎症途径,包括无粒细胞黏附和渗出、粒细胞黏附和渗出、IL-6 信号传导和 IL-10 信号传导,在神经变性和再生过程中持续激活。我们目前的研究扩展了我们对损伤后免疫/炎症相关途径改变的分子基础的理解,因此可能为将相关分子作为周围神经再生的治疗干预靶点提供可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0965/5405595/a9680360e943/MI2017-3827841.001.jpg

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